Reaction Details |
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Target | Dual specificity protein phosphatase 3 |
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Ligand | BDBM51780 |
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Substrate/Competitor | n/a |
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Meas. Tech. | uHTS absorbance assay for the identification of compounds that inhibit VHR1. |
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IC50 | 3970±n/a nM |
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Citation | PubChem, PC uHTS absorbance assay for the identification of compounds that inhibit VHR1. PubChem Bioassay(2009)[AID] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Dual specificity protein phosphatase 3 |
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Name: | Dual specificity protein phosphatase 3 |
Synonyms: | DUS3_HUMAN | DUSP3 | Dual specificity protein phosphatase (VHR) | Dual specificity protein phosphatase 3 | Dual specificity protein phosphatase VHR | Protein Tyrosine Phosphatase VHR | Tyrosine-protein phosphatase non-receptor type 1 | VHR |
Type: | Hydrolase |
Mol. Mass.: | 20480.58 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 185 |
Sequence: | MSGSFELSVQDLNDLLSDGSGCYSLPSQPCNEVTPRIYVGNASVAQDIPKLQKLGITHVL
NAAEGRSFMHVNTNANFYKDSGITYLGIKANDTQEFNLSAYFERAADFIDQALAQKNGRV
LVHCREGYSRSPTLVIAYLMMRQKMDVKSALSIVRQNREIGPNDGFLAQLCQLNDRLAKE
GKLKP
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BDBM51780 |
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n/a |
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Name | BDBM51780 |
Synonyms: | 5-[5-(6-Bromo-3-oxo-benzo[4,5]imidazo[2,1-b]thiazol-2-ylidenemethyl)-furan-2-yl]-2-chloro-benzoic acid | 5-[5-[(7-bromanyl-1-oxidanylidene-[1,3]thiazolo[3,2-a]benzimidazol-2-ylidene)methyl]furan-2-yl]-2-chloranyl-benzoic acid | 5-[5-[(7-bromo-1-keto-thiazolo[3,2-a]benzimidazol-2-ylidene)methyl]-2-furyl]-2-chloro-benzoic acid | 5-[5-[(7-bromo-1-oxo-2-thiazolo[3,2-a]benzimidazolylidene)methyl]-2-furanyl]-2-chlorobenzoic acid | 5-[5-[(7-bromo-1-oxo-[1,3]thiazolo[3,2-a]benzimidazol-2-ylidene)methyl]furan-2-yl]-2-chlorobenzoic acid | MLS001207823 | SMR000516642 | cid_3129904 |
Type | Small organic molecule |
Emp. Form. | C21H10BrClN2O4S |
Mol. Mass. | 501.737 |
SMILES | OC(=O)c1cc(ccc1Cl)-c1ccc(C=c2sc3nc4ccc(Br)cc4n3c2=O)o1 |
Structure |
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